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Chemical Structure| 109523-16-2 Chemical Structure| 109523-16-2

Structure of 109523-16-2

Chemical Structure| 109523-16-2

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Product Details of [ 109523-16-2 ]

CAS No. :109523-16-2
Formula : C13H21NO4
M.W : 255.31
SMILES Code : O=C([C@H]1N(C(OC(C)(C)C)=O)C2CCC1CC2)O
MDL No. :MFCD17016666

Safety of [ 109523-16-2 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338

Application In Synthesis of [ 109523-16-2 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 109523-16-2 ]

[ 109523-16-2 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 24424-99-5 ]
  • [ 109583-12-2 ]
  • [ 109523-16-2 ]
  • 2
  • [ 89466-16-0 ]
  • [ 109523-16-2 ]
  • (S)-tert-butyl 3-(6-bromo-3-methylpyridin-2-ylcarbamoyl)-2-azabicyclo[2.2.2]octane-2-carboxylate [ No CAS ]
YieldReaction ConditionsOperation in experiment
With N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline; N-ethyl-N,N-diisopropylamine; In dichloromethane; To a mixture of 3-Si (230 mg, 0.902 mmol), <strong>[89466-16-0]6-bromo-3-methylpyridin-2-amine</strong> (169 mg, 0.902 mmol), and EEDQ (446 mg, 1.80 mmol) in DCE(10 mL) was added DIPEA (0.6 mL, 3.61 mmol). The reaction mixture was stirred at 90 °C overnight. The mixture was then concentrated under reduced pressure and the remaining residue was purified by column chromatography on silica gel (eluted with PE/EtOAc = 20:1 to 10:1) to afford 3-S2 (100 mg, 26.2percent yield) as a yellow solid. LC/MS (ESI) m/z: 424 (M+H)t
 

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